Ab initio calculations show that the cyclic aromatic structure (hexaphosphabenzene) is a minimum on the Ps potential energy surface, and is kinetically stable to its unimolecular destruction. In contrast to the N, analogue, hexaphosphabenzene lies very close in energy to its valence Ps isomers. This
Stable and metastable photoexcitations of linear C−6. Theoretical study
✍ Scribed by Ludwik Adamowicz
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 463 KB
- Volume
- 182
- Category
- Article
- ISSN
- 0009-2614
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